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Comparison Of The Incidence Of Postoperative Pain Using Different Single File Systems: A Prospective, Randomized Clinical Trial

Comparison Of The Incidence Of Postoperative Pain After Using Different Single File Systems: A Prospective, Randomized Clinical Trial - PPSFS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2019/12/022402
Enrollment
150
Registered
2019-12-17
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

Dr Kriti Kapoor
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Mandibular molars of patients aged between 18 to 40 years with no systemic disease. 2.No history of trauma to the involved tooth. 3.No periapical radiolucency related to the involved tooth. 4.No parafunctional habit. 5.No pus or inflammatory exudate draining through the canal or sinus tract. 6.No tenderness on percussion in the involved tooth. 7.Positive response on cold testing and electric pulp testing.

Exclusion criteria

Exclusion criteria: 1.Patients with non-vital teeth. 2.Presence of sinus tracts or draining pus. 3.Cases of apical periodontitis. 4.Radiographic evidence of a periapical lesion. 5.Endodontic Retreatment cases. 6.Root resorption cases. 7.Immature or open apex cases 8.Root canal in which patency of apical foramen could not be established. 9.Patients whose teeth had issues precluding single visit treatment. 10.Teeth with anatomic variations and difficult root anatomy (canal curvatures >25 degree radiographic evidence of calcification. 11.Patients using some type of medication preoperatively such as analgesics or steroidal anti-inflammatory drugs. 12.Patients with any uncontrolled systemic diseases. 13.Patients with allergies to sodium hypochlorite. 14.Medically compromised patients. 15.Missing antagonist tooth. 16.Pregnant women. 17.Teeth with wide canals

Design outcomes

Primary

MeasureTime frame
To compare postoperative pain after root canal treatment using different single file systems .Timepoint: Pain assessment of the patient after 24 hrs,48 hrs, 72 hrs and 7 days—

Secondary

MeasureTime frame
Time taken for the treatment in every patient; Systemic analgesic intake of patient if anyTimepoint: Systemic analgesic intake of patient after 24 hrs,48 hrs,72 hrs and 7 days—

Countries

India

Contacts

Public ContactDr Mandeep S Grewal

SGT Dental College Hospital And Research Institute, Budhera Gurugram

drmandeepsgrewal@yahoo.co.in9810805880

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026